Risk Management Pharmacovigilance Specialist
Posted today by SciPro
SciPro are exclusively partnered with a leading, global pharmaceutical company with a culture of patient centricity, supporting their search for a Risk Management Pharmacovigilance Specialist. This role supports the QPPV office and DSPV functions on the oversight and finalization of RMP and RMMs as a subject matter expert within the EMEA PV team.
Within the role, you will ensure compliance with global PV regulations, lead effective implementation of local and regional RMPs with a critical mindset to continuously improve existing processes, whilst contributing to the development of new procedures in close collaboration with global stakeholders.
Key responsibilities:
- Support the finalization of RMPs and RMMs including relevant material.
- Assist Medical Safety leadership and MSLs with compliance oversight and tracking tool planning and oversight of RMP commitments.
- Support QPPV team in strategic impact assessment of PV regulations intelligence items.
Key Requirements:
- Knowledge of worldwide RMP regulations: prior experience with European Union (EU) regulations is required.
- Exposure to working relationships with regulatory authorities.
- Demonstrable, hands on experience of implementing local and regional RMPs
- Ability to independently lead long- and short-term project timelines and deliverables.
- Type:
- Permanent
- Contract Length:
- N/A
- Contact Name:
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- Telephone:
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- Job Reference:
- 281879_1727366408
- Job ID:
- 222389732
- Applications:
- Be first to apply
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